Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700034J05Rik |
T |
A |
6: 146,952,896 (GRCm38) |
D216V |
possibly damaging |
Het |
2610021A01Rik |
C |
T |
7: 41,626,657 (GRCm38) |
R595* |
probably null |
Het |
Adgrl3 |
A |
G |
5: 81,688,567 (GRCm38) |
D724G |
probably damaging |
Het |
Akap6 |
T |
C |
12: 53,140,795 (GRCm38) |
F1664S |
possibly damaging |
Het |
Akt1 |
T |
C |
12: 112,655,151 (GRCm38) |
I404V |
probably benign |
Het |
Anxa13 |
T |
A |
15: 58,341,948 (GRCm38) |
|
noncoding transcript |
Het |
Atoh1 |
T |
C |
6: 64,729,633 (GRCm38) |
V104A |
probably benign |
Het |
Brwd1 |
T |
C |
16: 96,021,237 (GRCm38) |
D1256G |
probably damaging |
Het |
C9 |
ATTTT |
ATTT |
15: 6,483,138 (GRCm38) |
|
probably null |
Het |
Cd164 |
A |
G |
10: 41,523,181 (GRCm38) |
T89A |
probably benign |
Het |
Cep350 |
G |
C |
1: 155,933,104 (GRCm38) |
N575K |
possibly damaging |
Het |
Chrm5 |
A |
G |
2: 112,480,252 (GRCm38) |
V173A |
probably damaging |
Het |
Cnot1 |
A |
G |
8: 95,741,944 (GRCm38) |
V1417A |
possibly damaging |
Het |
Cntnap3 |
T |
C |
13: 64,758,390 (GRCm38) |
T801A |
probably damaging |
Het |
Cntnap5b |
A |
C |
1: 100,072,140 (GRCm38) |
K208Q |
possibly damaging |
Het |
Crx |
A |
T |
7: 15,869,347 (GRCm38) |
V107D |
possibly damaging |
Het |
Csrnp2 |
A |
G |
15: 100,489,440 (GRCm38) |
F49S |
probably damaging |
Het |
Ctbp1 |
A |
G |
5: 33,250,904 (GRCm38) |
L228P |
possibly damaging |
Het |
Ctdp1 |
A |
T |
18: 80,449,401 (GRCm38) |
D626E |
possibly damaging |
Het |
Cyp1a2 |
T |
C |
9: 57,682,286 (GRCm38) |
T82A |
possibly damaging |
Het |
Dnah5 |
T |
C |
15: 28,343,591 (GRCm38) |
I2379T |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,092,192 (GRCm38) |
I2504T |
probably damaging |
Het |
Dnase1l2 |
A |
C |
17: 24,441,651 (GRCm38) |
W138G |
probably damaging |
Het |
Dopey2 |
T |
A |
16: 93,766,173 (GRCm38) |
I855N |
probably damaging |
Het |
Dsc3 |
T |
A |
18: 19,965,846 (GRCm38) |
N759Y |
possibly damaging |
Het |
Dtx2 |
C |
T |
5: 136,032,293 (GRCm38) |
R510* |
probably null |
Het |
Fat4 |
G |
T |
3: 38,887,115 (GRCm38) |
M52I |
probably benign |
Het |
Fat4 |
G |
A |
3: 38,996,090 (GRCm38) |
E4034K |
probably damaging |
Het |
Fezf2 |
T |
C |
14: 12,344,350 (GRCm38) |
K279R |
probably damaging |
Het |
Fsip2 |
G |
T |
2: 82,976,517 (GRCm38) |
W1060L |
possibly damaging |
Het |
G6pc |
T |
A |
11: 101,367,942 (GRCm38) |
I49N |
probably damaging |
Het |
Gars |
A |
G |
6: 55,077,772 (GRCm38) |
E688G |
probably null |
Het |
Gdf11 |
T |
C |
10: 128,885,242 (GRCm38) |
N361S |
probably benign |
Het |
Gli3 |
A |
C |
13: 15,726,380 (GRCm38) |
M1451L |
probably benign |
Het |
Heatr3 |
T |
C |
8: 88,150,317 (GRCm38) |
I329T |
probably benign |
Het |
Herc3 |
T |
G |
6: 58,884,975 (GRCm38) |
|
probably null |
Het |
Hrnr |
A |
G |
3: 93,332,604 (GRCm38) |
N3383S |
unknown |
Het |
Igsf3 |
A |
T |
3: 101,431,296 (GRCm38) |
I309F |
probably benign |
Het |
Kif21b |
C |
T |
1: 136,152,264 (GRCm38) |
R513W |
probably damaging |
Het |
Kif7 |
G |
T |
7: 79,699,241 (GRCm38) |
H1195Q |
probably benign |
Het |
Lpcat4 |
T |
C |
2: 112,242,542 (GRCm38) |
V182A |
possibly damaging |
Het |
Map3k21 |
T |
A |
8: 125,927,555 (GRCm38) |
I371N |
probably benign |
Het |
Mns1 |
G |
A |
9: 72,448,759 (GRCm38) |
|
probably null |
Het |
Myo3a |
A |
G |
2: 22,578,128 (GRCm38) |
T465A |
possibly damaging |
Het |
Nlrc4 |
A |
T |
17: 74,426,943 (GRCm38) |
S992T |
probably benign |
Het |
Notch4 |
G |
A |
17: 34,587,588 (GRCm38) |
G1833E |
possibly damaging |
Het |
Olfr160 |
A |
T |
9: 37,711,697 (GRCm38) |
I194K |
possibly damaging |
Het |
Olfr467 |
A |
T |
7: 107,814,700 (GRCm38) |
I39L |
probably benign |
Het |
Olfr600 |
T |
A |
7: 103,346,109 (GRCm38) |
Y273F |
possibly damaging |
Het |
Olfr666 |
T |
C |
7: 104,892,903 (GRCm38) |
T242A |
probably damaging |
Het |
Olfr998 |
G |
A |
2: 85,590,641 (GRCm38) |
V34I |
probably benign |
Het |
Pcdh9 |
G |
A |
14: 93,888,305 (GRCm38) |
P143L |
probably damaging |
Het |
Pik3cd |
T |
A |
4: 149,663,203 (GRCm38) |
T28S |
probably damaging |
Het |
Pkd1 |
G |
T |
17: 24,576,592 (GRCm38) |
|
probably null |
Het |
Plk4 |
A |
T |
3: 40,805,817 (GRCm38) |
S383C |
possibly damaging |
Het |
Plxna2 |
T |
C |
1: 194,643,989 (GRCm38) |
L77P |
probably damaging |
Het |
Ppm1f |
T |
C |
16: 16,923,666 (GRCm38) |
S335P |
probably damaging |
Het |
Prr16 |
C |
T |
18: 51,303,277 (GRCm38) |
P276L |
probably damaging |
Het |
Rilp |
A |
G |
11: 75,510,933 (GRCm38) |
|
probably null |
Het |
Rspry1 |
A |
G |
8: 94,632,054 (GRCm38) |
|
probably null |
Het |
Serpinb9b |
T |
C |
13: 33,029,559 (GRCm38) |
V33A |
probably benign |
Het |
Slc4a10 |
C |
A |
2: 62,268,204 (GRCm38) |
Q561K |
probably damaging |
Het |
Smyd5 |
T |
C |
6: 85,438,136 (GRCm38) |
I42T |
possibly damaging |
Het |
Stk17b |
T |
C |
1: 53,761,082 (GRCm38) |
N246D |
probably damaging |
Het |
Suco |
T |
C |
1: 161,818,811 (GRCm38) |
|
probably null |
Het |
Tcrg-C3 |
C |
A |
13: 19,260,994 (GRCm38) |
F37L |
probably damaging |
Het |
Tecpr1 |
C |
T |
5: 144,204,697 (GRCm38) |
V785M |
possibly damaging |
Het |
Telo2 |
C |
T |
17: 25,101,668 (GRCm38) |
V756I |
probably benign |
Het |
Tgm1 |
C |
T |
14: 55,705,577 (GRCm38) |
R602H |
probably benign |
Het |
Timeless |
A |
G |
10: 128,244,187 (GRCm38) |
T402A |
probably damaging |
Het |
Tnfaip2 |
T |
A |
12: 111,449,891 (GRCm38) |
|
probably null |
Het |
Trim5 |
A |
G |
7: 104,265,621 (GRCm38) |
S414P |
probably damaging |
Het |
Txnip |
A |
G |
3: 96,559,750 (GRCm38) |
T247A |
possibly damaging |
Het |
Vmn1r174 |
A |
T |
7: 23,754,625 (GRCm38) |
T239S |
probably damaging |
Het |
Vmn1r231 |
T |
A |
17: 20,889,950 (GRCm38) |
E234D |
probably damaging |
Het |
Zranb3 |
A |
T |
1: 127,959,743 (GRCm38) |
N982K |
probably benign |
Het |
|
Other mutations in Dnah3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00650:Dnah3
|
APN |
7 |
119,938,905 (GRCm38) |
missense |
possibly damaging |
0.88 |
IGL01095:Dnah3
|
APN |
7 |
119,951,597 (GRCm38) |
missense |
probably benign |
0.02 |
IGL01329:Dnah3
|
APN |
7 |
120,022,941 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01380:Dnah3
|
APN |
7 |
119,926,564 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01410:Dnah3
|
APN |
7 |
119,967,720 (GRCm38) |
missense |
possibly damaging |
0.91 |
IGL01487:Dnah3
|
APN |
7 |
119,965,530 (GRCm38) |
nonsense |
probably null |
|
IGL01843:Dnah3
|
APN |
7 |
119,943,575 (GRCm38) |
missense |
probably benign |
0.12 |
IGL01929:Dnah3
|
APN |
7 |
119,951,651 (GRCm38) |
nonsense |
probably null |
|
IGL01994:Dnah3
|
APN |
7 |
119,951,214 (GRCm38) |
missense |
possibly damaging |
0.58 |
IGL02115:Dnah3
|
APN |
7 |
120,029,054 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02273:Dnah3
|
APN |
7 |
119,951,271 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02299:Dnah3
|
APN |
7 |
119,967,579 (GRCm38) |
missense |
probably benign |
0.39 |
IGL02421:Dnah3
|
APN |
7 |
119,950,992 (GRCm38) |
missense |
possibly damaging |
0.87 |
IGL02514:Dnah3
|
APN |
7 |
119,966,247 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02596:Dnah3
|
APN |
7 |
119,938,914 (GRCm38) |
missense |
probably benign |
0.19 |
IGL02716:Dnah3
|
APN |
7 |
119,937,023 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL02738:Dnah3
|
APN |
7 |
119,965,497 (GRCm38) |
missense |
probably benign |
|
IGL03404:Dnah3
|
APN |
7 |
119,938,977 (GRCm38) |
missense |
probably damaging |
1.00 |
R0964_Dnah3_480
|
UTSW |
7 |
119,952,739 (GRCm38) |
splice site |
probably benign |
|
R1778_Dnah3_238
|
UTSW |
7 |
120,078,402 (GRCm38) |
missense |
probably damaging |
1.00 |
R4658_Dnah3_599
|
UTSW |
7 |
119,950,651 (GRCm38) |
missense |
probably damaging |
1.00 |
BB004:Dnah3
|
UTSW |
7 |
119,951,271 (GRCm38) |
missense |
probably damaging |
0.97 |
BB014:Dnah3
|
UTSW |
7 |
119,951,271 (GRCm38) |
missense |
probably damaging |
0.97 |
R0011:Dnah3
|
UTSW |
7 |
120,019,701 (GRCm38) |
missense |
probably damaging |
1.00 |
R0195:Dnah3
|
UTSW |
7 |
120,077,775 (GRCm38) |
critical splice donor site |
probably null |
|
R0241:Dnah3
|
UTSW |
7 |
119,922,730 (GRCm38) |
missense |
probably damaging |
1.00 |
R0241:Dnah3
|
UTSW |
7 |
119,922,730 (GRCm38) |
missense |
probably damaging |
1.00 |
R0312:Dnah3
|
UTSW |
7 |
120,045,659 (GRCm38) |
missense |
probably damaging |
1.00 |
R0316:Dnah3
|
UTSW |
7 |
119,965,659 (GRCm38) |
missense |
possibly damaging |
0.94 |
R0370:Dnah3
|
UTSW |
7 |
120,086,720 (GRCm38) |
missense |
possibly damaging |
0.91 |
R0426:Dnah3
|
UTSW |
7 |
119,943,572 (GRCm38) |
missense |
probably benign |
0.11 |
R0525:Dnah3
|
UTSW |
7 |
119,928,754 (GRCm38) |
missense |
probably damaging |
1.00 |
R0625:Dnah3
|
UTSW |
7 |
120,071,887 (GRCm38) |
missense |
possibly damaging |
0.68 |
R0627:Dnah3
|
UTSW |
7 |
120,020,915 (GRCm38) |
missense |
probably damaging |
1.00 |
R0632:Dnah3
|
UTSW |
7 |
119,967,905 (GRCm38) |
missense |
probably benign |
0.11 |
R0928:Dnah3
|
UTSW |
7 |
120,030,051 (GRCm38) |
missense |
probably damaging |
1.00 |
R0964:Dnah3
|
UTSW |
7 |
119,952,739 (GRCm38) |
splice site |
probably benign |
|
R0972:Dnah3
|
UTSW |
7 |
120,035,340 (GRCm38) |
splice site |
probably null |
|
R1066:Dnah3
|
UTSW |
7 |
120,061,009 (GRCm38) |
missense |
probably damaging |
1.00 |
R1082:Dnah3
|
UTSW |
7 |
120,078,445 (GRCm38) |
missense |
probably damaging |
1.00 |
R1127:Dnah3
|
UTSW |
7 |
119,923,030 (GRCm38) |
missense |
probably damaging |
1.00 |
R1132:Dnah3
|
UTSW |
7 |
119,939,004 (GRCm38) |
missense |
possibly damaging |
0.50 |
R1222:Dnah3
|
UTSW |
7 |
120,090,676 (GRCm38) |
missense |
probably benign |
0.28 |
R1420:Dnah3
|
UTSW |
7 |
119,951,979 (GRCm38) |
missense |
probably damaging |
0.99 |
R1456:Dnah3
|
UTSW |
7 |
120,047,630 (GRCm38) |
missense |
probably damaging |
1.00 |
R1472:Dnah3
|
UTSW |
7 |
120,070,958 (GRCm38) |
missense |
probably benign |
0.12 |
R1617:Dnah3
|
UTSW |
7 |
120,089,946 (GRCm38) |
missense |
probably benign |
0.01 |
R1624:Dnah3
|
UTSW |
7 |
120,019,695 (GRCm38) |
missense |
probably damaging |
0.99 |
R1654:Dnah3
|
UTSW |
7 |
119,926,449 (GRCm38) |
missense |
probably damaging |
1.00 |
R1673:Dnah3
|
UTSW |
7 |
119,971,179 (GRCm38) |
nonsense |
probably null |
|
R1677:Dnah3
|
UTSW |
7 |
119,928,740 (GRCm38) |
missense |
probably damaging |
1.00 |
R1687:Dnah3
|
UTSW |
7 |
120,045,786 (GRCm38) |
splice site |
probably null |
|
R1711:Dnah3
|
UTSW |
7 |
120,078,571 (GRCm38) |
missense |
probably damaging |
1.00 |
R1738:Dnah3
|
UTSW |
7 |
120,035,359 (GRCm38) |
missense |
probably damaging |
1.00 |
R1778:Dnah3
|
UTSW |
7 |
120,078,402 (GRCm38) |
missense |
probably damaging |
1.00 |
R1866:Dnah3
|
UTSW |
7 |
119,928,856 (GRCm38) |
splice site |
probably null |
|
R1883:Dnah3
|
UTSW |
7 |
120,077,919 (GRCm38) |
missense |
probably benign |
0.06 |
R1894:Dnah3
|
UTSW |
7 |
120,086,334 (GRCm38) |
missense |
probably benign |
0.05 |
R1929:Dnah3
|
UTSW |
7 |
119,975,129 (GRCm38) |
missense |
probably benign |
0.10 |
R1988:Dnah3
|
UTSW |
7 |
119,967,959 (GRCm38) |
missense |
probably damaging |
0.99 |
R2010:Dnah3
|
UTSW |
7 |
120,095,177 (GRCm38) |
start codon destroyed |
probably benign |
0.00 |
R2022:Dnah3
|
UTSW |
7 |
119,951,242 (GRCm38) |
missense |
probably damaging |
1.00 |
R2026:Dnah3
|
UTSW |
7 |
120,039,406 (GRCm38) |
missense |
probably damaging |
1.00 |
R2063:Dnah3
|
UTSW |
7 |
119,951,909 (GRCm38) |
missense |
probably damaging |
0.96 |
R2131:Dnah3
|
UTSW |
7 |
119,967,759 (GRCm38) |
missense |
possibly damaging |
0.93 |
R2152:Dnah3
|
UTSW |
7 |
119,952,013 (GRCm38) |
missense |
probably benign |
0.02 |
R2199:Dnah3
|
UTSW |
7 |
119,951,569 (GRCm38) |
missense |
possibly damaging |
0.89 |
R2271:Dnah3
|
UTSW |
7 |
119,975,129 (GRCm38) |
missense |
probably benign |
0.10 |
R2350:Dnah3
|
UTSW |
7 |
120,045,788 (GRCm38) |
splice site |
probably null |
|
R2567:Dnah3
|
UTSW |
7 |
119,952,697 (GRCm38) |
missense |
possibly damaging |
0.83 |
R2848:Dnah3
|
UTSW |
7 |
119,967,938 (GRCm38) |
missense |
probably benign |
0.01 |
R2902:Dnah3
|
UTSW |
7 |
119,951,499 (GRCm38) |
missense |
possibly damaging |
0.61 |
R2926:Dnah3
|
UTSW |
7 |
119,951,115 (GRCm38) |
missense |
probably damaging |
1.00 |
R2944:Dnah3
|
UTSW |
7 |
119,951,110 (GRCm38) |
missense |
probably damaging |
1.00 |
R3022:Dnah3
|
UTSW |
7 |
120,078,481 (GRCm38) |
missense |
possibly damaging |
0.93 |
R3401:Dnah3
|
UTSW |
7 |
119,967,656 (GRCm38) |
missense |
probably benign |
0.00 |
R3402:Dnah3
|
UTSW |
7 |
119,967,656 (GRCm38) |
missense |
probably benign |
0.00 |
R3403:Dnah3
|
UTSW |
7 |
119,967,656 (GRCm38) |
missense |
probably benign |
0.00 |
R3919:Dnah3
|
UTSW |
7 |
119,951,080 (GRCm38) |
missense |
probably damaging |
1.00 |
R3972:Dnah3
|
UTSW |
7 |
120,086,720 (GRCm38) |
missense |
probably damaging |
0.99 |
R4162:Dnah3
|
UTSW |
7 |
119,922,838 (GRCm38) |
missense |
probably damaging |
1.00 |
R4184:Dnah3
|
UTSW |
7 |
120,083,293 (GRCm38) |
missense |
probably damaging |
1.00 |
R4198:Dnah3
|
UTSW |
7 |
119,922,838 (GRCm38) |
missense |
probably damaging |
1.00 |
R4199:Dnah3
|
UTSW |
7 |
119,922,838 (GRCm38) |
missense |
probably damaging |
1.00 |
R4200:Dnah3
|
UTSW |
7 |
119,922,838 (GRCm38) |
missense |
probably damaging |
1.00 |
R4239:Dnah3
|
UTSW |
7 |
120,029,025 (GRCm38) |
nonsense |
probably null |
|
R4478:Dnah3
|
UTSW |
7 |
120,071,863 (GRCm38) |
missense |
probably benign |
0.00 |
R4579:Dnah3
|
UTSW |
7 |
120,009,331 (GRCm38) |
missense |
probably damaging |
1.00 |
R4600:Dnah3
|
UTSW |
7 |
120,089,946 (GRCm38) |
missense |
probably benign |
|
R4649:Dnah3
|
UTSW |
7 |
120,047,698 (GRCm38) |
missense |
probably damaging |
1.00 |
R4658:Dnah3
|
UTSW |
7 |
119,950,651 (GRCm38) |
missense |
probably damaging |
1.00 |
R4728:Dnah3
|
UTSW |
7 |
120,059,366 (GRCm38) |
missense |
probably damaging |
0.99 |
R4739:Dnah3
|
UTSW |
7 |
120,077,946 (GRCm38) |
missense |
possibly damaging |
0.54 |
R4758:Dnah3
|
UTSW |
7 |
120,079,406 (GRCm38) |
missense |
probably benign |
0.00 |
R4785:Dnah3
|
UTSW |
7 |
119,967,824 (GRCm38) |
missense |
probably benign |
0.29 |
R4789:Dnah3
|
UTSW |
7 |
120,011,072 (GRCm38) |
missense |
probably damaging |
1.00 |
R4930:Dnah3
|
UTSW |
7 |
119,951,681 (GRCm38) |
nonsense |
probably null |
|
R4935:Dnah3
|
UTSW |
7 |
120,016,477 (GRCm38) |
nonsense |
probably null |
|
R4946:Dnah3
|
UTSW |
7 |
119,931,560 (GRCm38) |
missense |
probably damaging |
1.00 |
R4981:Dnah3
|
UTSW |
7 |
119,956,201 (GRCm38) |
missense |
probably benign |
0.03 |
R4984:Dnah3
|
UTSW |
7 |
119,928,779 (GRCm38) |
missense |
probably benign |
0.04 |
R5025:Dnah3
|
UTSW |
7 |
120,071,905 (GRCm38) |
missense |
probably benign |
0.02 |
R5046:Dnah3
|
UTSW |
7 |
119,951,580 (GRCm38) |
missense |
probably damaging |
1.00 |
R5056:Dnah3
|
UTSW |
7 |
120,020,946 (GRCm38) |
missense |
probably damaging |
1.00 |
R5068:Dnah3
|
UTSW |
7 |
120,032,790 (GRCm38) |
missense |
probably benign |
|
R5069:Dnah3
|
UTSW |
7 |
120,032,790 (GRCm38) |
missense |
probably benign |
|
R5154:Dnah3
|
UTSW |
7 |
119,952,419 (GRCm38) |
missense |
probably damaging |
1.00 |
R5208:Dnah3
|
UTSW |
7 |
120,032,638 (GRCm38) |
missense |
probably damaging |
1.00 |
R5323:Dnah3
|
UTSW |
7 |
120,021,011 (GRCm38) |
missense |
probably damaging |
1.00 |
R5330:Dnah3
|
UTSW |
7 |
119,943,648 (GRCm38) |
missense |
probably benign |
0.00 |
R5385:Dnah3
|
UTSW |
7 |
119,924,903 (GRCm38) |
missense |
probably damaging |
1.00 |
R5391:Dnah3
|
UTSW |
7 |
120,090,076 (GRCm38) |
missense |
probably benign |
0.02 |
R5564:Dnah3
|
UTSW |
7 |
119,971,466 (GRCm38) |
critical splice donor site |
probably null |
|
R5594:Dnah3
|
UTSW |
7 |
119,971,621 (GRCm38) |
missense |
possibly damaging |
0.89 |
R5610:Dnah3
|
UTSW |
7 |
119,939,065 (GRCm38) |
splice site |
probably null |
|
R5673:Dnah3
|
UTSW |
7 |
119,951,589 (GRCm38) |
missense |
possibly damaging |
0.91 |
R5678:Dnah3
|
UTSW |
7 |
120,077,851 (GRCm38) |
missense |
probably benign |
0.00 |
R5737:Dnah3
|
UTSW |
7 |
120,059,198 (GRCm38) |
missense |
probably benign |
0.03 |
R5766:Dnah3
|
UTSW |
7 |
119,978,222 (GRCm38) |
missense |
probably damaging |
1.00 |
R5769:Dnah3
|
UTSW |
7 |
120,089,952 (GRCm38) |
nonsense |
probably null |
|
R5789:Dnah3
|
UTSW |
7 |
119,943,599 (GRCm38) |
missense |
possibly damaging |
0.70 |
R5791:Dnah3
|
UTSW |
7 |
119,931,473 (GRCm38) |
missense |
probably benign |
0.00 |
R5841:Dnah3
|
UTSW |
7 |
119,951,021 (GRCm38) |
utr 3 prime |
probably benign |
|
R5843:Dnah3
|
UTSW |
7 |
119,951,021 (GRCm38) |
utr 3 prime |
probably benign |
|
R5844:Dnah3
|
UTSW |
7 |
119,951,021 (GRCm38) |
utr 3 prime |
probably benign |
|
R5846:Dnah3
|
UTSW |
7 |
119,951,021 (GRCm38) |
utr 3 prime |
probably benign |
|
R5851:Dnah3
|
UTSW |
7 |
120,039,362 (GRCm38) |
missense |
possibly damaging |
0.51 |
R5853:Dnah3
|
UTSW |
7 |
119,938,833 (GRCm38) |
missense |
probably damaging |
1.00 |
R5857:Dnah3
|
UTSW |
7 |
119,951,021 (GRCm38) |
utr 3 prime |
probably benign |
|
R5865:Dnah3
|
UTSW |
7 |
119,975,108 (GRCm38) |
missense |
probably benign |
0.00 |
R5885:Dnah3
|
UTSW |
7 |
120,069,704 (GRCm38) |
missense |
probably benign |
0.10 |
R5898:Dnah3
|
UTSW |
7 |
120,078,501 (GRCm38) |
missense |
probably benign |
0.37 |
R5917:Dnah3
|
UTSW |
7 |
120,016,526 (GRCm38) |
missense |
probably damaging |
1.00 |
R5964:Dnah3
|
UTSW |
7 |
119,922,880 (GRCm38) |
missense |
probably benign |
0.00 |
R5990:Dnah3
|
UTSW |
7 |
120,073,541 (GRCm38) |
missense |
probably benign |
|
R6004:Dnah3
|
UTSW |
7 |
120,086,297 (GRCm38) |
missense |
probably benign |
0.10 |
R6033:Dnah3
|
UTSW |
7 |
120,071,647 (GRCm38) |
missense |
probably benign |
0.00 |
R6033:Dnah3
|
UTSW |
7 |
120,071,647 (GRCm38) |
missense |
probably benign |
0.00 |
R6045:Dnah3
|
UTSW |
7 |
119,967,522 (GRCm38) |
missense |
probably damaging |
0.99 |
R6056:Dnah3
|
UTSW |
7 |
120,030,031 (GRCm38) |
missense |
probably damaging |
1.00 |
R6133:Dnah3
|
UTSW |
7 |
120,086,246 (GRCm38) |
missense |
probably benign |
0.10 |
R6229:Dnah3
|
UTSW |
7 |
119,965,488 (GRCm38) |
missense |
probably benign |
0.11 |
R6237:Dnah3
|
UTSW |
7 |
120,009,384 (GRCm38) |
missense |
probably damaging |
1.00 |
R6333:Dnah3
|
UTSW |
7 |
120,054,633 (GRCm38) |
missense |
probably damaging |
1.00 |
R6408:Dnah3
|
UTSW |
7 |
119,922,968 (GRCm38) |
splice site |
probably null |
|
R6447:Dnah3
|
UTSW |
7 |
119,923,054 (GRCm38) |
missense |
probably benign |
0.12 |
R6606:Dnah3
|
UTSW |
7 |
120,060,956 (GRCm38) |
missense |
probably benign |
0.02 |
R6666:Dnah3
|
UTSW |
7 |
120,070,949 (GRCm38) |
missense |
probably benign |
0.16 |
R6733:Dnah3
|
UTSW |
7 |
119,922,974 (GRCm38) |
missense |
probably benign |
0.22 |
R6815:Dnah3
|
UTSW |
7 |
119,971,727 (GRCm38) |
missense |
probably benign |
|
R6882:Dnah3
|
UTSW |
7 |
119,971,184 (GRCm38) |
missense |
possibly damaging |
0.95 |
R6934:Dnah3
|
UTSW |
7 |
120,054,601 (GRCm38) |
critical splice donor site |
probably null |
|
R6966:Dnah3
|
UTSW |
7 |
120,032,754 (GRCm38) |
missense |
probably damaging |
1.00 |
R7025:Dnah3
|
UTSW |
7 |
120,030,010 (GRCm38) |
missense |
possibly damaging |
0.90 |
R7207:Dnah3
|
UTSW |
7 |
119,971,089 (GRCm38) |
missense |
probably damaging |
1.00 |
R7214:Dnah3
|
UTSW |
7 |
119,922,742 (GRCm38) |
missense |
probably damaging |
1.00 |
R7222:Dnah3
|
UTSW |
7 |
120,071,523 (GRCm38) |
missense |
probably benign |
0.00 |
R7235:Dnah3
|
UTSW |
7 |
120,032,670 (GRCm38) |
missense |
probably damaging |
1.00 |
R7241:Dnah3
|
UTSW |
7 |
119,943,633 (GRCm38) |
missense |
probably benign |
0.03 |
R7313:Dnah3
|
UTSW |
7 |
119,981,344 (GRCm38) |
missense |
probably benign |
0.39 |
R7342:Dnah3
|
UTSW |
7 |
120,029,985 (GRCm38) |
missense |
probably damaging |
1.00 |
R7368:Dnah3
|
UTSW |
7 |
120,029,016 (GRCm38) |
missense |
probably benign |
|
R7375:Dnah3
|
UTSW |
7 |
119,951,677 (GRCm38) |
missense |
probably damaging |
1.00 |
R7395:Dnah3
|
UTSW |
7 |
120,060,960 (GRCm38) |
missense |
probably benign |
0.00 |
R7395:Dnah3
|
UTSW |
7 |
119,966,251 (GRCm38) |
missense |
|
|
R7431:Dnah3
|
UTSW |
7 |
120,051,744 (GRCm38) |
missense |
probably damaging |
1.00 |
R7499:Dnah3
|
UTSW |
7 |
120,060,912 (GRCm38) |
missense |
probably damaging |
0.99 |
R7515:Dnah3
|
UTSW |
7 |
120,073,592 (GRCm38) |
missense |
probably benign |
0.21 |
R7564:Dnah3
|
UTSW |
7 |
119,971,594 (GRCm38) |
missense |
probably benign |
|
R7618:Dnah3
|
UTSW |
7 |
119,978,378 (GRCm38) |
missense |
probably damaging |
0.97 |
R7697:Dnah3
|
UTSW |
7 |
119,967,434 (GRCm38) |
missense |
|
|
R7728:Dnah3
|
UTSW |
7 |
119,938,828 (GRCm38) |
missense |
probably damaging |
1.00 |
R7757:Dnah3
|
UTSW |
7 |
119,971,215 (GRCm38) |
splice site |
probably null |
|
R7757:Dnah3
|
UTSW |
7 |
120,071,570 (GRCm38) |
missense |
probably benign |
|
R7774:Dnah3
|
UTSW |
7 |
119,951,752 (GRCm38) |
nonsense |
probably null |
|
R7804:Dnah3
|
UTSW |
7 |
120,011,012 (GRCm38) |
missense |
probably damaging |
1.00 |
R7804:Dnah3
|
UTSW |
7 |
119,952,618 (GRCm38) |
missense |
probably damaging |
1.00 |
R7857:Dnah3
|
UTSW |
7 |
119,951,704 (GRCm38) |
missense |
probably damaging |
1.00 |
R7871:Dnah3
|
UTSW |
7 |
119,967,552 (GRCm38) |
missense |
|
|
R7903:Dnah3
|
UTSW |
7 |
120,042,128 (GRCm38) |
missense |
probably damaging |
1.00 |
R7927:Dnah3
|
UTSW |
7 |
119,951,271 (GRCm38) |
missense |
probably damaging |
0.97 |
R7989:Dnah3
|
UTSW |
7 |
120,077,789 (GRCm38) |
missense |
probably benign |
|
R8142:Dnah3
|
UTSW |
7 |
120,060,966 (GRCm38) |
missense |
probably benign |
0.00 |
R8164:Dnah3
|
UTSW |
7 |
119,967,614 (GRCm38) |
missense |
probably damaging |
1.00 |
R8237:Dnah3
|
UTSW |
7 |
119,926,413 (GRCm38) |
missense |
probably benign |
0.01 |
R8313:Dnah3
|
UTSW |
7 |
119,951,152 (GRCm38) |
missense |
probably benign |
0.38 |
R8338:Dnah3
|
UTSW |
7 |
120,071,881 (GRCm38) |
missense |
probably benign |
0.01 |
R8355:Dnah3
|
UTSW |
7 |
119,952,208 (GRCm38) |
missense |
probably damaging |
1.00 |
R8408:Dnah3
|
UTSW |
7 |
119,952,505 (GRCm38) |
missense |
probably damaging |
1.00 |
R8411:Dnah3
|
UTSW |
7 |
120,011,030 (GRCm38) |
missense |
probably damaging |
1.00 |
R8455:Dnah3
|
UTSW |
7 |
119,952,208 (GRCm38) |
missense |
probably damaging |
1.00 |
R8483:Dnah3
|
UTSW |
7 |
119,937,030 (GRCm38) |
missense |
probably benign |
0.00 |
R8531:Dnah3
|
UTSW |
7 |
119,951,368 (GRCm38) |
missense |
probably damaging |
1.00 |
R8885:Dnah3
|
UTSW |
7 |
119,962,152 (GRCm38) |
missense |
|
|
R8912:Dnah3
|
UTSW |
7 |
120,090,646 (GRCm38) |
missense |
probably benign |
0.06 |
R8966:Dnah3
|
UTSW |
7 |
119,950,658 (GRCm38) |
nonsense |
probably null |
|
R8982:Dnah3
|
UTSW |
7 |
119,937,071 (GRCm38) |
missense |
probably damaging |
1.00 |
R9043:Dnah3
|
UTSW |
7 |
119,952,049 (GRCm38) |
missense |
probably benign |
|
R9053:Dnah3
|
UTSW |
7 |
120,019,764 (GRCm38) |
missense |
possibly damaging |
0.67 |
R9059:Dnah3
|
UTSW |
7 |
120,085,145 (GRCm38) |
missense |
probably benign |
0.01 |
R9182:Dnah3
|
UTSW |
7 |
120,085,128 (GRCm38) |
missense |
probably damaging |
0.98 |
R9365:Dnah3
|
UTSW |
7 |
119,967,636 (GRCm38) |
missense |
|
|
R9383:Dnah3
|
UTSW |
7 |
120,047,596 (GRCm38) |
missense |
probably benign |
0.23 |
R9430:Dnah3
|
UTSW |
7 |
120,028,982 (GRCm38) |
missense |
probably damaging |
1.00 |
R9449:Dnah3
|
UTSW |
7 |
119,952,250 (GRCm38) |
missense |
probably benign |
0.12 |
R9462:Dnah3
|
UTSW |
7 |
119,952,300 (GRCm38) |
missense |
probably benign |
0.05 |
R9505:Dnah3
|
UTSW |
7 |
120,045,689 (GRCm38) |
missense |
probably damaging |
1.00 |
R9559:Dnah3
|
UTSW |
7 |
120,051,728 (GRCm38) |
missense |
probably benign |
0.07 |
R9562:Dnah3
|
UTSW |
7 |
120,010,891 (GRCm38) |
missense |
probably benign |
0.05 |
R9565:Dnah3
|
UTSW |
7 |
120,010,891 (GRCm38) |
missense |
probably benign |
0.05 |
R9609:Dnah3
|
UTSW |
7 |
120,071,013 (GRCm38) |
missense |
probably damaging |
0.98 |
R9622:Dnah3
|
UTSW |
7 |
119,962,133 (GRCm38) |
missense |
|
|
R9633:Dnah3
|
UTSW |
7 |
119,950,993 (GRCm38) |
missense |
probably benign |
|
R9654:Dnah3
|
UTSW |
7 |
120,042,173 (GRCm38) |
nonsense |
probably null |
|
R9665:Dnah3
|
UTSW |
7 |
120,045,758 (GRCm38) |
missense |
probably benign |
0.01 |
R9681:Dnah3
|
UTSW |
7 |
120,078,388 (GRCm38) |
missense |
probably benign |
0.04 |
R9717:Dnah3
|
UTSW |
7 |
119,975,076 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1088:Dnah3
|
UTSW |
7 |
120,010,873 (GRCm38) |
missense |
probably null |
1.00 |
Z1088:Dnah3
|
UTSW |
7 |
120,086,297 (GRCm38) |
missense |
probably benign |
0.00 |
Z1176:Dnah3
|
UTSW |
7 |
119,967,803 (GRCm38) |
missense |
|
|
Z1177:Dnah3
|
UTSW |
7 |
120,007,862 (GRCm38) |
missense |
probably benign |
|
Z1177:Dnah3
|
UTSW |
7 |
119,967,901 (GRCm38) |
missense |
probably damaging |
0.99 |
|